Rainbow Rare Earths Phalaborwa project shaping up to be one of the lowest cost producers globally. Watch the video here.
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Been researching the Bluechew pills online as I have seen the advertisements on a large number of podcasts/youtube channels recently and wanted to understand how it compares to FUM.
https://www.healthline.com/health/all-about-bluechew#pros-and-cons
From the above link it states that Bluechew isn't actually approved by the FDA but all the active ingredients have been (i.e. Sildenafil and Tadalafil). Given FUM have no active ingredients, anyone have any ideas as to why FUM cannot also market and sell the product now prior to FDA approval just like Bluechew are?
I think it will be sold in the USA via online from abroad for starters.
These are just generic Viagra.
Sorry they are branded generic Viagra and Cialis . We are selling Eroxon as a medical device so need FDA approval.
Helloclouds - I understand all the active ingredients are already FDA approved (i.e. Cialis/Viagra) and all Bluechew have added are the additional non-active ingredients to make it chewable/faster acting but I don't understand why they can still sell when the final product hasn't been approved when FUM's product contains NO active ingredients and yet they need to await approval?
Hedgefundking - could be right, perhaps the product being made abroad changes the approval process?
It doesn't change the approval process but as it is not a drug it will fin its way into the USA via Ebay,amazon marketplace and a whole host of other online stores.
The reason I flagged Mexico is that huge amounts of prescription drugs are available OTC there and huge amounts of those find their way into the USA.
As this is an OTC product I am sure there will be alot of product finding its way over the border and quite legally too.
Liambooth - interesting that you consider those links as negative on FUM.
The fact they agreed to authorise the use of unlicensed MED2002 on the NHS to me shows a need for the product and a clear gap in the market. They wouldn't approve it if the existing approved products covered the same requirements
Didn't agree to anything? You even read your own links? Literally says the NHS Business Services Authority has agreed that MED2002 will be reimbursed by the NHS.
Add to that the definition of specials:
Specials are medicines that have not been authorised and which are requested and prescribed for the treatment on a named patient basis only by appropriately qualified doctors under their own authority. Such requests can only be made subject to a number of conditions being met including the absence of licensed alternatives.
Absence of licensed alternatives, literally what I said. You've provided a link, I have written back to you what is in that link and now you are seemingly disagreeing with me while at the same time agreeing? I'm very confused....
Yeah thats it, "invested outside their circle of competence and understanding".
Been posting on here since the price was 15p and its now 50p, more than tripled my money in 3 months but I clearly lack the competence or understanding.
You've been getting a load of flack on here and generally I'm not against people giving a negative opinion if its informed. Unfortunately what I am learning from you during this brief discussion is that you literally ignore 90% of a conversation, pick a tiny technicality (and what you are saying couldn't even be described as that) and jump on it, copy and paste a load of sentences to think you are super smart then get personal. That link was CLEARLY not negative for FUM, it literally refers to 7% of the market that only FUM's product can work for and that's why it was given special status.
Honestly if you are more than 20 years old you should be embarrassed. You sound like such a child who thinks that knowing how to copy and paste makes them smart. Truly truly embarrassing
Regarding Liam
https://www.change.org/p/australian-public-stop-dishonest-practices-on-the-australian-stock-exchange-and-demand-a-royal-commission/u/27309590?fbclid=IwAR1vY31HnOL3ZouCAmBT76Hj942-Wmdx6N3IoUcf_a27kh0XxE1dLRN2wEI
Anyone who hasn't seen this should check it out.
Well lesson learn't there! Seemingly I am now one of the few people on here to bother to engage in a conversation with him and I won't be making that mistake again.
Just very strange to come onto a forum of a company where the majority of contributors have been very successful and made a lot of money and suggest they are incompetent, he knows so much that others don't and that people generally don't know what they are doing/investing in.
Bothers me how much time I spent engaging with him, feels like such a waste of time so beggars belief how he can find the energy to argue with people he doesn't know and will never meet seemingly multiple times every day
@ LBO
But healthcare professionals need to be made aware of the availability of the special product and need to be reminded. It takes anywhere from 4-8 sales interactions before an HCP changes how they prescribe, some won't do it unless a colleague has prescribed a new medicine and had decent patient feedback.
This is not a cheap process , that's why sales and marketing expenses are a big part of pharma companies balance sheets. I guess Futura made the decision that the revenue from specials wouldn't be worth the sales and marketing expense.
Wilco - I'm sure the pill packaging must use components or contain excipients that already approved by the FDA so combined with an approved generic they would just need to get a registration dossier approved to show they can provide the product to standard.
As they are loads of ED "products" with no clinical trail backup , Futura are seeking to differentiate by having medical device status hence why they are waiting for approval.
Cheers for the response Helloclouds.
So the Healthline article in my original post was slightly misleading in that Bluechew will never seek FDA approval and therefore it shouldn't be considered a "con" that approval hasn't yet been received?
81Lucky thanks for that post.I have been saying it all along.
Here is an extract from that article. Sounds familiar?
here are three types of bashers here at Global Calumny Funds:
Advanced, Intermediate and Beginner. An Advanced-level basher (also
known as a Silver Tongued Devil) would spread false or misleading
information about the company.
They would deal in facts, countering every longs post with articles,
news reports and opinion surveys that gave a negative impression about
the company.
An Intermediate-level basher (also known as a Serpent) would try to
weasel their way into the confidence of longs and create doubt using
rumor or innuendo.
Finally, a Beginner-level basher (also known as a Pitchfork) would
attempt to create confusion in the room by distracting other posters
with satire, name calling and pointless arguments. The idea was to
make sure no serious discussion of the stock
could take place.
Wilco - exactly. they are a branded generic so they have to show some differentiation ( mode of delivery - chewy rather than pill ) and it's mainly way they are selling it - Loads of marketing spend and a inertia sell ( looks like you get a pack of pills a month unless you cancel) .
@wilco999 12:50
You're not the first petson to try and have a logical conversation with Mr (Team?) Booth.
Nor are you the first to point out how some of his links don't actually back up the arguments he makes. But hey they look good; strongly worded sentences with links underneath.
But it's always worth doing your own DD and checking the sources of others, and if your anything like me you end up being more confident about the company. I mean why would someone go to such long lengths to spread FUD? I have my answer, I'll leave everyone else to come to their own conclusions.